ENST00000262367.10:c.5173-138C>G
MANE Select
|
ENSP00000262367.5:n.5173-138C>G
|
|
ENST00000262367.9:c.5173-138C>G
|
ENSP00000262367.5:n.5173-138C>G
|
|
ENST00000382070.7:c.5059-138C>G
|
ENSP00000371502.3:n.5059-138C>G
|
|
NM_001079846.1:c.5059-138C>G
|
NP_001073315.1:n.5059-138C>G
|
|
NM_004380.2:c.5173-138C>G
|
NP_004371.2:n.5173-138C>G
|
|
XM_005255124.3:c.5128-138C>G
|
XP_005255181.1:n.5128-138C>G
|
|
XM_005255125.3:c.4756-138C>G
|
XP_005255182.1:n.4756-138C>G
|
|
XM_006720848.2:c.4912-138C>G
|
XP_006720911.1:n.4912-138C>G
|
|
XM_011522380.1:c.5119-138C>G
|
XP_011520682.1:n.5119-138C>G
|
|
XM_011522381.1:c.4420-138C>G
|
XP_011520683.1:n.4420-138C>G
|
|
XM_005255124.4:c.5128-138C>G
|
XP_005255181.1:n.5128-138C>G
|
|
XM_005255125.4:c.4756-138C>G
|
XP_005255182.1:n.4756-138C>G
|
|
XM_006720848.3:c.4912-138C>G
|
XP_006720911.1:n.4912-138C>G
|
|
XM_011522381.2:c.4420-138C>G
|
XP_011520683.1:n.4420-138C>G
|
|
XM_017022944.1:c.5167-138C>G
|
XP_016878433.1:n.5167-138C>G
|
|
NM_004380.3:c.5173-138C>G
MANE Select
|
NP_004371.2:n.5173-138C>G
|
|